Canonical Allele Identifier: CA378314377

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247533T>G (hg19) ; chr10:g.121488019T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488019T>G , CM000672.2:g.121488019T>G	GRCh38
NC_000010.10:g.123247533T>G , CM000672.1:g.123247533T>G	GRCh37
NC_000010.9:g.123237523T>G	NCBI36
NG_012449.1:g.115440A>C
NG_012449.2:g.115440A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1961A>C MANE Plus Clinical	ENSP00000410294.2:p.Asn654Thr
ENST00000351936.11:c.1952A>C	ENSP00000309878.10:p.Asn651Thr
ENST00000638709.2:c.782A>C	ENSP00000491912.2:p.Asn261Thr
ENST00000682296.1:n.1300A>C
ENST00000682550.1:c.1607A>C	ENSP00000507633.1:p.Asn536Thr
ENST00000682772.1:c.782A>C	ENSP00000506848.1:p.Asn261Thr
ENST00000682904.1:n.778A>C
ENST00000683029.1:n.370A>C
ENST00000683211.1:c.1952A>C	ENSP00000508257.1:p.Asn651Thr
ENST00000683250.1:c.*660A>C	ENSP00000506847.1:n.*660A>C
ENST00000683418.1:n.4299A>C
ENST00000684153.1:c.1607A>C	ENSP00000506937.1:p.Asn536Thr
ENST00000684516.1:n.2971A>C
ENST00000358487.10:c.1958A>C MANE Select	ENSP00000351276.6:p.Asn653Thr
ENST00000336553.10:c.1685A>C	ENSP00000337665.6:p.Asn562Thr
ENST00000346997.6:c.1952A>C	ENSP00000263451.5:p.Asn651Thr
ENST00000351936.10:c.1958A>C	ENSP00000309878.9:p.Asn653Thr
ENST00000356226.8:c.1607A>C	ENSP00000348559.4:p.Asn536Thr
ENST00000357555.9:c.1691A>C	ENSP00000350166.5:p.Asn564Thr
ENST00000358487.9:c.1958A>C	ENSP00000351276.5:p.Asn653Thr
ENST00000360144.7:c.1694A>C	ENSP00000353262.3:p.Asn565Thr
ENST00000369056.5:c.1961A>C	ENSP00000358052.1:p.Asn654Thr
ENST00000369058.7:c.1961A>C	ENSP00000358054.3:p.Asn654Thr
ENST00000369059.5:c.1616A>C	ENSP00000358055.1:p.Asn539Thr
ENST00000369060.8:c.1610A>C	ENSP00000358056.4:p.Asn537Thr
ENST00000369061.8:c.1622A>C	ENSP00000358057.4:p.Asn541Thr
ENST00000429361.5:c.734A>C	ENSP00000404219.1:p.Asn245Thr
ENST00000457416.6:c.1961A>C	ENSP00000410294.2:p.Asn654Thr
ENST00000478859.5:c.1274A>C	ENSP00000474011.1:p.Asn425Thr
ENST00000604236.5:c.*1005A>C	ENSP00000474109.1:n.*1005A>C
ENST00000613048.4:c.1691A>C	ENSP00000484154.1:p.Asn564Thr
NM_000141.4:c.1958A>C	NP_000132.3:p.Asn653Thr
NM_001144913.1:c.1961A>C	NP_001138385.1:p.Asn654Thr
NM_001144914.1:c.1622A>C	NP_001138386.1:p.Asn541Thr
NM_001144915.1:c.1691A>C	NP_001138387.1:p.Asn564Thr
NM_001144916.1:c.1613A>C	NP_001138388.1:p.Asn538Thr
NM_001144917.1:c.1610A>C	NP_001138389.1:p.Asn537Thr
NM_001144918.1:c.1607A>C	NP_001138390.1:p.Asn536Thr
NM_001144919.1:c.1694A>C	NP_001138391.1:p.Asn565Thr
NM_022970.3:c.1961A>C	NP_075259.4:p.Asn654Thr
NM_023029.2:c.1691A>C	NP_075418.1:p.Asn564Thr
NR_073009.1:n.2408A>C
XM_006717708.2:c.2012A>C	XP_006717771.1:p.Asn671Thr
XM_006717709.2:c.2009A>C	XP_006717772.1:p.Asn670Thr
XM_006717710.2:c.2018A>C	XP_006717773.1:p.Asn673Thr
XM_006717711.2:c.1751A>C	XP_006717774.1:p.Asn584Thr
XM_006717712.2:c.1673A>C	XP_006717775.1:p.Asn558Thr
XM_006717713.2:c.2015A>C	XP_006717776.1:p.Asn672Thr
XM_011539510.1:c.1274A>C	XP_011537812.1:p.Asn425Thr
NM_001320654.1:c.1274A>C	NP_001307583.1:p.Asn425Thr
NM_001320658.1:c.1952A>C	NP_001307587.1:p.Asn651Thr
XM_006717708.3:c.2012A>C	XP_006717771.1:p.Asn671Thr
XM_006717710.4:c.2018A>C	XP_006717773.1:p.Asn673Thr
XM_017015920.2:c.2012A>C	XP_016871409.1:p.Asn671Thr
XM_017015921.2:c.2009A>C	XP_016871410.1:p.Asn670Thr
XM_017015924.2:c.1670A>C	XP_016871413.1:p.Asn557Thr
XM_017015925.2:c.1664A>C	XP_016871414.1:p.Asn555Thr
XM_024447887.1:c.1748A>C	XP_024303655.1:p.Asn583Thr
XM_024447888.1:c.1745A>C	XP_024303656.1:p.Asn582Thr
XM_024447889.1:c.1742A>C	XP_024303657.1:p.Asn581Thr
XM_024447890.1:c.1751A>C	XP_024303658.1:p.Asn584Thr
XM_024447891.1:c.1673A>C	XP_024303659.1:p.Asn558Thr
XM_024447892.1:c.788A>C	XP_024303660.1:p.Asn263Thr
NM_000141.5:c.1958A>C MANE Select	NP_000132.3:p.Asn653Thr
NM_001144917.2:c.1610A>C	NP_001138389.1:p.Asn537Thr
NM_001144918.2:c.1607A>C	NP_001138390.1:p.Asn536Thr
NM_001144919.2:c.1694A>C	NP_001138391.1:p.Asn565Thr
NM_001320658.2:c.1952A>C	NP_001307587.1:p.Asn651Thr
NR_073009.2:n.2394A>C
NM_001144915.2:c.1691A>C	NP_001138387.1:p.Asn564Thr
NM_001144916.2:c.1613A>C	NP_001138388.1:p.Asn538Thr
NM_001320654.2:c.1274A>C	NP_001307583.1:p.Asn425Thr